Yan Qidong, Gao Shang, Zhang Xianglun, Liu Guoping, Chen Peitao, Gao Xuanyi, Yuan Li, Tian Yucheng, Li Dapeng, Zhang Xuepeng, Zhang Huan
Key Laboratory of Sweet Potato Biology and Biotechnology, Ministry of Agriculture and Rural Affairs/Beijing Key Laboratory of Crop Genetic Improvement/Laboratory of Crop Heterosis & Utilization and Joint Laboratory for International Cooperation in Crop Molecular Breeding, Ministry of Education, College of Agronomy & Biotechnology, China Agricultural University, Beijing 100193, China.
Shandong Academy of Agricultural Sciences, Jinan 250100, China.
Genes (Basel). 2024 Dec 19;15(12):1628. doi: 10.3390/genes15121628.
and have obvious morphological features and strongly tolerate saline-alkali environments. However, the mechanisms that lead to the differences in saline-alkali tolerance between them remain unclear.
In this study, we employed comparative transcriptome analysis to investigate and under saline-alkali stress.
Our sequencing efforts resulted in the identification of 99,868 unigenes. We obtained 12,021 and 6227 differentially expressed genes (DEGs) from the and under salt stress compared with plants in the control. Notably, 1189 and 1864 were specifically upregulated DEGs in the roots and leaves of under saline-alkali conditions, respectively. These genes were enriched in pathways such as "Plant hormone signal transduction", "Carbon metabolism" and "Starch and sucrose metabolism". Further analysis of stress-related pathways and gene expression levels revealed that key genes involved in abscisic acid (ABA) and jasmonic acid (JA) biosynthesis, ABA signal transduction, and their downstream transcription factors were upregulated in the roots of under saline-alkali conditions. Additionally, 24 DEGs associated with stress response were identified in the roots and leaves of both species. The expression levels of these pathways and related genes were higher in than in , suggesting that enhances its saline-alkali tolerance by elevating the expression of these genes.
This study provides a new research perspective for revealing the differences in saline-alkali tolerance mechanisms between and , bringing forth important candidate genes for studying their saline-alkali tolerance.
[物种1]和[物种2]具有明显的形态特征,并且对盐碱环境具有很强的耐受性。然而,导致它们之间耐盐碱差异的机制仍不清楚。
在本研究中,我们采用比较转录组分析来研究盐碱胁迫下的[物种1]和[物种2]。
我们的测序工作共鉴定出99,868个单基因。与对照植株相比,在盐胁迫下,我们从[物种1]和[物种2]中分别获得了12,021个和6227个差异表达基因(DEG)。值得注意的是,在盐碱条件下,[物种1]的根和叶中分别有1189个和1864个DEG特异性上调。这些基因富集在“植物激素信号转导”、“碳代谢”和“淀粉和蔗糖代谢”等途径中。对胁迫相关途径和基因表达水平的进一步分析表明,参与脱落酸(ABA)和茉莉酸(JA)生物合成、ABA信号转导及其下游转录因子的关键基因在盐碱条件下[物种1]的根中上调。此外,在两个物种的根和叶中均鉴定出24个与胁迫反应相关的DEG。这些途径和相关基因在[物种1]中的表达水平高于[物种2],表明[物种1]通过提高这些基因的表达来增强其耐盐碱能力。
本研究为揭示[物种1]和[物种2]耐盐碱机制的差异提供了新的研究视角,为研究它们的耐盐碱能力带来了重要的候选基因。